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t(10;11)(p12.3;q23.3)

MedGen UID:
1713273
•Concept ID:
C5238353
•
Cell or Molecular Dysfunction

Definition

A cytogenetic abnormality that refers to the translocation of the short arm (p12.3) of chromosome 10 and the long arm (q23.3) of chromosome 11. It is associated with KMT2A (MLL) fusions and acute myeloid leukemia. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVt(10;11)(p12.3;q23.3)

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